Attend the Maiva Pharma walk-in interview on August 3, 2025, for roles in sterile injectable production, FR&D, QA, QC, and engineering. Join a USFDA-approved facility in Hosur and build your pharmaceutical career.
Maiva Pharma Walk-In Interview – Sterile Injectables Careers on August 3, 2025
Looking to advance your pharmaceutical career with a globally recognized sterile injectable manufacturer? Maiva Pharma Pvt. Ltd., a USFDA and EU-GMP certified company, is inviting experienced professionals for a walk-in interview in Bangalore on Sunday, August 3, 2025. Explore rewarding roles in Production, FR&D, QA, QC, and Engineering for our state-of-the-art manufacturing facility in Hosur, Tamil Nadu.
🏭 About Maiva Pharma
Established in 1996, Maiva Pharma is a reputed contract development and manufacturing organization (CDMO) specializing in sterile injectables. With global regulatory approvals including USFDA, EU-GMP, and more, Maiva serves major pharmaceutical markets in the USA, Europe, Canada, and Australia. The company is known for its adherence to quality, operational excellence, and innovation in lyophilized and aseptic formulations.
📅 Walk-In Interview Details
- Date: Sunday, August 3, 2025
- Time: 9:00 AM – 4:00 PM
- Venue: Sai Vishram Business Hotel, 144/C1, Kirloskar Road, Bommasandra Industrial Area, Hebbagodi, Bangalore – 560099
- Work Location: Maiva Pharma Pvt. Ltd., No. 32, SIPCOT Industrial Complex, Phase I, Hosur, Tamil Nadu – 635126
📌 Mandatory Documents: Resume, educational certificates, Aadhaar, PAN, increment letter, 3 months’ payslips, relieving/service certificates
💼 Open Positions and Eligibility
🔹 Production (Injectables)
- Qualification: M.Pharm, B.Pharm, B.Tech, M.Tech (Pharmaceutical Eng.)
- Experience: 2–10 years
- Key Skills: Aseptic operations, vial washing & filling, compounding, sealing, lyophilization, autoclave operations
🔹 FR&D / Tech Transfer
- Qualification: M.Pharm, B.Pharm, B.Tech, M.Tech
- Experience: 2–10 years
- Key Skills: Sterile formulation development, process validation, scale-up, exhibit batches, R&D
🔹 Process Engineering / QMS
- Qualification: BE (EEE, Mech, ECE, E&I)
- Experience: 3–10 years
- Key Skills: Vial filling line maintenance, lyophilizer handling, autoclave validation, sterile area QMS
🔹 Quality Control (Chemical)
- Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc
- Experience: 2–5 years
- Key Skills: HPLC, GC, UV, IR, water analysis, finished & raw material testing, stability studies
🔹 Quality Assurance
- Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc
- Experience: 2–7 years
- Key Skills: IPQA, BMR/BPR, QMS, validation (PV & CV), batch release
🌟 Why Work at Maiva Pharma?
✅ USFDA & EU-GMP Facility – Work in a globally compliant plant
✅ Career Growth Opportunities – Learn, lead, and grow in sterile manufacturing
✅ Innovative R&D Environment – Be part of critical injectable product development
✅ Employee Satisfaction – Rated 3.9/5 on AmbitionBox based on 90+ reviews
✅ Global Exposure – Contribute to over 75 products in regulated markets
📧 How to Apply
- Attend in person on August 3, 2025, at the venue
- Or email your resume to hr@maivapharma.com with the subject line: [Department] Application – August 2025
🛡️ Note on Fraud Prevention
Maiva Pharma does NOT charge fees for recruitment. Beware of unauthorized job offers from unofficial emails (like Gmail/Yahoo). For any concerns, write to info@maivapharma.com.
💡 Tips for Applicants
- ✔️ Prepare a clear resume highlighting sterile injectable experience
- ✔️ Review your expertise in HPLC, GC, lyophilization, and aseptic processes
- ✔️ Study Maiva’s global certifications and product pipeline
- ✔️ Be ready for shift-based work and cGMP audits
🔬 Build Your Future in Sterile Injectables
A career in sterile injectables promises high stability, regulatory exposure, and international opportunities. If you’re passionate about pharma manufacturing excellence, this is your time to shine.
Join Maiva Pharma – Let’s make Pharma. Made Better. a reality.
